psyc 390 CH 1 rev lecture Flashcards

(53 cards)

1
Q

Movement of a drug from the site of administration to the circulatory system

A

absorption

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2
Q

Rapid tolerance formed during a single administration of a drug as is the case with alcohol

A

acute tolerance

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3
Q

Drug interactions characterized by the collective sum of the two individual drug effects

A

additive effects

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4
Q

Area in the medulla of the brain stem that is not isolated from chemicals in the blood It is responsible for inducing a vomiting response when a toxic substance is present in the blood

A

area postrema

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5
Q

Starshaped cells of the nerve tissue that have numerous extensions and that modulate the chemical environment around neurons metabolically assist neurons and provide phagocytosis for cellular debris

A

astrocytes

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6
Q

The reduced effectiveness of a drug administered chronically that involves learning either instumental or classical conditioning

A

behavioral tolerance

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7
Q

Concentration of drug present in the blood that is free to bind to specific target sites

A

bioavailability

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8
Q

Inactivation of a drug through a chemical change usually by metabolic processes in the liver

A

biotransformation

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9
Q

Drug that binds to a receptor but has little or no efficacy When it competes with an agonist for receptor sites it reduces the effect of the agonist

A

competitive antagonist

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10
Q

Difference in the amount or concentration of a substance on each side of a biological barrier such as the cell membrane

A

concentration gradient

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11
Q

Tolerance to a specific drug can reduce the effectiveness of a another drug in the same class

A

crosstolerance

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12
Q

Type of drug interaction involving binding to an inactive site such as to proteins in the plasma to bone or to fat

A

depot binding

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13
Q

Graph used to display the amount of biological change in relation to a given drug dose

A

dose response curve

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14
Q

Decrease in the number of receptors which may be a consequence of chronic agonist treatment

A

downregulation

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15
Q

Molecular changes associated with a drug binding to a particular target site or receptor

A

drug action

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16
Q

Interaction between two drugs that share a metabolic system and compete for the same metabolic enzymes Bioavailability of one or both increases

A

drug competition

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17
Q

Inactive sites where drugs accumulate There is no biological effect from drugs binding at these sites nor can they be metabolized

A

drug depots

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18
Q

Alterations in physiological or psychological functions associated with a specific drug

A

drug effects

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19
Q

The extent to which a ligandreceptor binding initiates a biological action eg the ability of an agonist to activate its receptor

A

efficacy

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20
Q

Term used to describe exponential elimination of drugs from the bloodstream

A

first order kinetics

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21
Q

Phenomenon in which the liver metabolizes some of a drug before it can circulate through the body particularly when the drug has been taken orally

A

first pass metabolism

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22
Q

Substance that activates a receptor but produces the opposite effect of a typical agonist at that receptor

A

inverse agonist

23
Q

Process involving the dissociation of an electrically neutral molecule into charged particles ions

24
Q

Molecule that selectively binds to a receptor

25
Type of tolerance to a drug that is characterized by a reduced amount of drug available at the target tissue often as a result of morerapid drug metabolism It is sometimes also called drug disposition tolerance
metabolic tolerance
26
Area of pharmacology specializing in druginduced changes to the function of cells in the nervous system
neuropharmacology
27
Area of pharmacology focusing on chemical substances that interact with the nervous system to alter behavior emotions and cognition
neuropsychopharmacology
28
Drug that reduces the effect of an agonist but does not compete at the receptor site The drug may bind to an inactive portion of the receptor disturb the cell membrane around the receptor or interrupt the intercellular processes initiated by the agonist receptor association
noncompetitive antagonist
29
Physical or behavioral changes not associated with the chemical activity of the drug receptor interaction but with certain unique characteristics of the individual such as present mood or expectations of drug effects
nonspecific drug effects
30
Type of learning in which animals learn to repond to obtain rewards and avoid punishment
operant conditioning
31
Drugs that bind to a receptor but have low efficacy producing weaker biological effects than a full agonist Hence they act as agonists at some receptors and antagonists at others depending on the regional concentration of full agonist These were previously called mixed agonistantagonists
partial agonists
32
Movement of lipidsoluble materials across a biological barrier without assistance based on its concentration gradient from higher to lower concentration
passive diffusion
33
Study of physiological and biochemical interactions of a drug with the target tissue responsible for the drugs effects
pharmacodynamics
34
The study of the genetic basis for variability in drug response among individuals sometimes called pharmacogenomics
pharmacogenetics
35
Factors that contribute to bioavailability the administration absorption distribution binding inactivation and excretion of a drug
pharmacokinetic
36
Study of the actions of drugs and their effects on living organisms
pharmacology
37
Drug interaction characterized by two drugs reducing each others effectiveness in the body
physiological antagonism
38
Drug interaction characterized by an increase in effectiveness greater than the collective sum of the individual drugs
potentiation
39
Those drugs that have an effect on thinking mood or behavior
psychoactive drugs
40
Area of pharmacology specializing in druginduced changes in mood thinking and behavior
psychopharmacology
41
A neurochemical or drug that can bind to a particular receptor protein and alter the shape of the receptor to initiate a cellular response
receptor agonist
42
A molecule that interacts with a receptor protein and produces no cellular effect after binding and also prevents an active ligand from binding
receptor antagonist
43
Group of receptors that respond to the same neurotransmitter but that differ from each other to varying degrees with respect to their structure signaling mechanisms and pharmacology
receptor subtypes
44
Proteins located on the surface of or within cells that bind to specific ligands to initiate biological changes within the cell
receptors
45
Enhanced response to a particular drug after repeated drug exposure
sensitization
46
Physical or behavioral changes associated with biochemical interactions of a drug with the target site
specific drug effects
47
Condition characterized by better performance of a particular task that was learned in a drugged state in the same drugged state rather than in a nondrugged state Tasks learned in a nondrugged state are likewise performed better in a nondrugged state
statedependent learning
48
Taking multiple blood samples to directly measure plasma levels of a drug after administration to identify the optimum dosage for maximum therapeutic potential and minimal side effects
therapeutic drug monitoring
49
Desired physical or behavioral changes associated with a particular drug
therapeutic effects
50
The relationship between the drug dose that results in a toxic response compared to the dose required for the desired biological response It is represented by the equation TI TD50ED50 where TD50 is the dose that is toxic for 50% of the population and ED50 is the effective dose for 50%
therapeutic index
51
Decreased response to a drug as a direct result of repeated drug exposure
tolerance
52
Increase in the number of receptors which may be a consequence of denervation or of chronic antagonist treatment
upregulation
53
Term used to describe a constant rate of drug removal from the body regardless of drug concentration in the blood
zero order kinetics